Abstract |
The potency and duration of action of a single dose of etintidine, ranitidine and cimetidine were compared in placebo-controlled studies. In addition, the effect of a single night-time dose of etintidine (600 mg) on gastric acid secretion and basal hormone levels was assessed before, during and after a 28-day treatment. Nocturnal gastric acidity (23.00-07.00) was inhibited from 41.04 +/- 5.0 mmol/l to 12.9 +/- 2.8 mmol/l by 300 mg etintidine, to 6.50 +/- 2.5 mmol/l by 600 mg etintidine and to 8.58 +/- 2.5 mmol/l by 800 mg cimetidine nocte. Etintidine and cimetidine did not reduce H+-concentrations during the following day. Pentagastrin-stimulated acid output was virtually not affected after 600 mg etintidine and 800 mg cimetidine as well. By contrast, stimulated acid secretion was still suppressed by about 50% following 300 mg ranitidine. Basal levels of testosterone, prolactin etc. remained unchanged by 28-day etintidine (600 mg dose at night) treatment. Clinical studies are needed to examine the place of the single dose of etintidine (600 mg) at night for the short-term treatment of duodenal ulcer.
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Authors | P Müller, H G Dammann, B Simon |
Journal | Zeitschrift fur Gastroenterologie
(Z Gastroenterol)
Vol. 23
Issue 3
Pg. 115-20
(Mar 1985)
ISSN: 0044-2771 [Print] Germany |
Vernacular Title | Einmal abendliche Gabe von Etintidin beim Menschen: Wirkung auf Süresekretion und Verhalten wichtiger Hormone. |
PMID | 2867653
(Publication Type: Clinical Trial, Comparative Study, Controlled Clinical Trial, Journal Article)
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Chemical References |
- Gastrins
- Histamine H2 Antagonists
- Hormones
- Imidazoles
- Cimetidine
- Ranitidine
- etintidine
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Topics |
- Adult
- Cimetidine
(pharmacology)
- Clinical Trials as Topic
- Double-Blind Method
- Drug Administration Schedule
- Gastric Acid
(metabolism)
- Gastric Acidity Determination
- Gastrins
(blood)
- Histamine H2 Antagonists
(pharmacology)
- Hormones
(blood)
- Humans
- Imidazoles
(pharmacology)
- Male
- Ranitidine
(pharmacology)
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